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Synthesis of ZrO2:Pr3+,Gd3+ nanocrystals for optical thermometry with a thermal sensitivity above 2.32% K−1 over 270 K of sensing range.

Authors :
Li, Minghui
Zhou, Jun
Lei, Ruoshan
Wang, Huanping
Huang, Feifei
Xu, Shiqing
Source :
Dalton Transactions: An International Journal of Inorganic Chemistry. 11/21/2021, Vol. 50 Issue 43, p15688-15695. 8p.
Publication Year :
2021

Abstract

Nowadays, there is enthusiastic effort to develop luminescent thermometers used for remote and high-sensitivity temperature readout over a wide sensing range. Herein, Pr3+ and Gd3+ co-doped ZrO2 nanocrystals are designed, prepared and investigated by XRD, Raman spectroscopy, XPS, TEM, EDS, DRS, PLE and PL spectroscopy. Upon 275 nm irradiation, the PL spectrum of ZrO2:Pr3+,Gd3+ is found to be composed of a narrow emission peak at 314 nm (Gd3+ 6P7/2–8S7/2), a broad defect-related emission band at 400 nm, and several emission peaks in the wavelength region of 585–700 nm (Pr3+ 1D2–3H4, 3P0–3H6, and 3P0–3F2), which exhibit different thermal responses owing to the effects of the various non-radiative relaxation processes and trap energy levels. Accordingly, the luminescence intensity ratio (LIR) between the Pr3+ 1D2–3H4 and Gd3+ 6P7/2–8S7/2 transitions demonstrates excellent relative sensing sensitivity values ((2.32 ± 0.01)% K−1–(8.32 ± 0.05)% K−1) and low temperature uncertainties (0.08 K–0.28 K) over a wide temperature sensing range of 303 K to 573 K, which are remarkably better than those of many other luminescence thermometers. What is discussed in the present study may be conducive to broadening the research region of RE3+ doped luminescence thermometric phosphors, especially for materials with rich 4f–4f transition lines and defect-related luminescence. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14779226
Volume :
50
Issue :
43
Database :
Academic Search Index
Journal :
Dalton Transactions: An International Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
154435388
Full Text :
https://doi.org/10.1039/d1dt02070f